ClinVar Miner

Submissions for variant NM_004998.4(MYO1E):c.2673A>G (p.Ala891=)

gnomAD frequency: 0.26773  dbSNP: rs2306791
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001512482 SCV001719909 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001512482 SCV001846615 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001779225 SCV002015881 benign Focal segmental glomerulosclerosis 6 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001512482 SCV005289522 benign not provided criteria provided, single submitter not provided

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